A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936055



Internal ID24751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73687218..73687963hg38UCSC Ensembl
chr3:73736369..73737114hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38746
hg19746
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438556
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936055
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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